Peter Winther Commerou

Nordic Medical Science Liaison, Reproductive Medicine at IBSA Nordic Aps
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Contact Information
us****@****om
(386) 825-5501
Location
Copenhagen, Capital Region, Denmark, DK
Languages
  • Danish Native or bilingual proficiency
  • English Full professional proficiency

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Credentials

  • Good Clinical Practice Course
    National Institutes of Health
    Nov, 2014
    - Oct, 2024

Experience

    • Nordic Medical Science Liaison, Reproductive Medicine
      • Apr 2021 - Present

      Medical responsible for the Nordic region within our four TA's including Reproductive Medicine, Urology, Endocrinology and Rheumatology. - Setting up scientific collaborations - RWE generation - Maintain a KOL-network across the Nordics - Setup and execution of advisory boards both nationally and Nordic - Apart of the global medical task force generating material for all our affiliates Medical responsible for the Nordic region within our four TA's including Reproductive Medicine, Urology, Endocrinology and Rheumatology. - Setting up scientific collaborations - RWE generation - Maintain a KOL-network across the Nordics - Setup and execution of advisory boards both nationally and Nordic - Apart of the global medical task force generating material for all our affiliates

    • Switzerland
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Medical Science Liaison, Opthalmology
      • Jul 2019 - Mar 2021

      Build external scientific partnerships with healthcare professionals and other decision makers to strategically prepare and support the development, launch and commercialization of our drug products. Provide fair balanced scientific information and education about products, clinical trials, and scientific activities within Ophthalmology. Build external scientific partnerships with healthcare professionals and other decision makers to strategically prepare and support the development, launch and commercialization of our drug products. Provide fair balanced scientific information and education about products, clinical trials, and scientific activities within Ophthalmology.

    • Switzerland
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Clinical Trial Manager
      • Oct 2016 - Mar 2019

      Drive clinical trial management with the clinical team, ensuring trial startup, sponsor oversight, risk-based monitoring setup, site-audits, stakeholder management, contract negotiations and communication.- Managing of five multi-national clinical trials (Phase II-IV) across Europe, USA and Denmark.- Contract negotiations with trial sites and relevant external stakeholders.- Implementation of processes ensuring Adverse Event reporting and Central Laboratory processes are working as intended.- Drive training of HCPs in different therapeutic areas. - Drive internal and external communication to HCPs at sites, CRO and internal stakeholders.- Therapeutic Area: Reproductive Health (Fertility), Clinical Care (Sepsis) & Oncology (Prostate Cancer) Show less

    • International Clinical Trial Coordinator
      • Aug 2016 - Oct 2016

      Drive clinical trial management along with the rest of the clinical team, ensuring trial progression and targets were met.- Responsible for implementation and execution of sponsor oversight activities.- Drive training and communication for relevant HCPs- Therapeutic Area: Clinical Care (Sepsis)

    • Clinical Research Assosicate
      • Dec 2014 - Jul 2016

      Ensuring data quality and trial progression at trial sites, including on-site and centralized monitoring activities, site-initiation, close-out visits, procedural optimization, training of monitors and maintaining strong working relationships with relevant HCPs. - Monitoring of four multi-national clinical trials (Phase II-III) across Denmark and USA - Extensive communication with relevant HCPs and maintenance of working relationships - Deep understanding of clinical operations setup - Therapeutic Area: Rheumatology (Osteoarthritis, Osteoporosis & Rheumatoid Arthritis) Show less

    • India
    • Construction
    • 1 - 100 Employee
    • Master Thesis Student
      • Feb 2013 - Feb 2014

      Worked with monitoring within clinical trials - on the focus and outcome of present procedures and how they could be improved.Gathered data from a first-in-man study over a period of 6 months, where i was present for the monitoring visits and audit.Keywords: Monitoring, Clinical Trials, SOPs and ICH-GCP

    • Student Worker
      • Feb 2013 - Aug 2013

      Sorting patent applications and documentation for product registration

    • Denmark
    • Armed Forces
    • 700 & Above Employee
    • Gardehusar
      • Aug 2013 - Dec 2013

      Soldiering Soldiering

Education

  • Københavns Universitet
    Master's Degree, Pharmaceutical Sciences
    2011 - 2014
  • Roskilde University
    B.Sc., Molecular biology and Medicinal biology
    2007 - 2011
  • HTX Naestved
    Student exam, Chemistry, Biology and Health
    2002 - 2005

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